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AA06550

1016847-66-7 | 1-(3-Bromophenyl)piperidin-2-one

Packsize Purity Availability Price Discounted Price    Quantity
250mg 96% in stock $48.00 $34.00 -   +
1g 96% in stock $128.00 $90.00 -   +
5g 96% in stock $413.00 $290.00 -   +
25g 96% in stock $1,536.00 $1,075.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA06550
Chemical Name: 1-(3-Bromophenyl)piperidin-2-one
CAS Number: 1016847-66-7
Molecular Formula: C11H12BrNO
Molecular Weight: 254.1230800000001
MDL Number: MFCD04037063
SMILES: Brc1cccc(c1)N1CCCCC1=O

 

Computed Properties
Complexity: 219  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 2.4  

 

 

Upstream Synthesis Route
  • 1-(3-Bromophenyl)piperidin-2-one, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely used in pharmaceutical research and development due to its unique structure and properties. With its distinctive piperidinone moiety and bromophenyl group, $name$ serves as a key intermediate in the synthesis of various bioactive compounds and pharmaceuticals.In the field of medicinal chemistry, 1-(3-Bromophenyl)piperidin-2-one is utilized as a valuable precursor for the preparation of novel drug candidates. Its structural features make it a valuable starting material for the synthesis of heterocyclic compounds and complex organic molecules. By introducing functional groups or modifying the piperidinone ring, chemists can tailor the properties of the final products, leading to the discovery of potential new drugs with enhanced biological activities.Furthermore, the bromophenyl substituent in $name$ imparts additional reactivity and versatility to the molecule. This allows for further derivatization and diversification through cross-coupling reactions, halogenation, or other synthetic transformations. The presence of the bromine atom enables chemists to introduce stereochemical diversity and modulate the physicochemical properties of the target molecules, making it a valuable tool in drug discovery and medicinal chemistry research.Overall, the application of 1-(3-Bromophenyl)piperidin-2-one in chemical synthesis extends beyond its role as a simple building block. Its strategic placement within molecular frameworks and its ability to undergo various synthetic manipulations make it an indispensable component in the development of pharmaceuticals and bioactive compounds.
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